HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Long non-coding RNA NEAT1 promotes colorectal cancer progression by competitively binding miR-34a with SIRT1 and enhancing the Wnt/β-catenin signaling pathway.

Abstract
In recent years, accumulating evidence has indicated that long non-coding RNAs (lncRNAs) are powerful factors influencing the progression of multiple malignancies. Although a relationship between the lncRNA NEAT1 (nuclear enriched abundant transcript 1) and colorectal cancer has previously been reported, the functional mechanism underlying the involvement of NEAT1 in colorectal cancer remains unknown. In this study, we report that NEAT1 expression is up-regulated in colorectal cancer tissues, which correlates with advanced clinical features, poor overall survival and disease free survival. Up-regulated NEAT1 promotes cell proliferation and metastasis of colorectal cancer both in vitro and in vivo. Moreover, NEAT1 functions as an oncogene influencing cell viability and invasion in part by serving as a competing endogenous RNA (ceRNAs) modulating miRNA-34a expression, leading to subsequent repression of the miR-34a/SIRT1 axis and activation of the Wnt/β-catenin signaling pathway. Taken together, our study demonstrates that the lncRNA NEAT1 may serve as a prognostic biomarker and a potential therapeutic target in colorectal cancer.
AuthorsYang Luo, Jian-Jun Chen, Qiang Lv, Jun Qin, Yi-Zhou Huang, Min-Hao Yu, Ming Zhong
JournalCancer letters (Cancer Lett) Vol. 440-441 Pg. 11-22 (01 2019) ISSN: 1872-7980 [Electronic] Ireland
PMID30312725 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2018 Elsevier B.V. All rights reserved.
Chemical References
  • CTNNB1 protein, human
  • MIRN34 microRNA, human
  • MicroRNAs
  • NEAT1 long non-coding RNA, human
  • RNA, Long Noncoding
  • beta Catenin
  • SIRT1 protein, human
  • Sirtuin 1
Topics
  • Aged
  • Animals
  • Binding, Competitive
  • Caco-2 Cells
  • Cell Line, Tumor
  • Colorectal Neoplasms (genetics, metabolism)
  • Female
  • HCT116 Cells
  • HT29 Cells
  • Heterografts
  • Humans
  • Male
  • Mice, Inbred BALB C
  • Mice, Nude
  • MicroRNAs (metabolism)
  • Middle Aged
  • RNA, Long Noncoding (genetics, metabolism)
  • Sirtuin 1 (metabolism)
  • Up-Regulation
  • Wnt Signaling Pathway
  • beta Catenin (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: